Prostatic ductal system in rats: regional variation in morphological and functional activities
The rat prostate is a complex ductal system with branches and subbranches extending from one end to another. Owing to the relative distance of various regions of the duct from the urethra, the entire length of the ductal system can be arbitrarily divided into three segments, i.e., the proximal, inte...
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Veröffentlicht in: | Biology of reproduction 1990-12, Vol.43 (6), p.1079-1086 |
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Zusammenfassung: | The rat prostate is a complex ductal system with branches and subbranches extending from one end to another. Owing to the
relative distance of various regions of the duct from the urethra, the entire length of the ductal system can be arbitrarily
divided into three segments, i.e., the proximal, intermediate, and distal segments. The present study was carried out to assess
the regional variation in cellular activities in this ductal system. Ventral prostates from adult Sprague-Dawley rats were
dissected so that an individual ductal system was mechanically isolated and longitudinally sectioned to reveal various segments.
Epithelial cells lining distal segments were tall-columnar type and were actively engaging in mitotic activity. Cells in intermediate
segments were also tall-columnar type. However, they were mitotically quiescent, but able to produce secretory proteins. Evidence
of programmed cell death was not observed in either of these two segments. Cells in proximal segments, on the other hand,
were low-columnar or cuboidal in shape and were stained heavily for cathepsin D, a marker associated with late manifestation
of cell death. Following castration in adult rats, there was a reversal in the site of programmed death in cells lining the
ductal system. By Day 4 post-castration, distal segments contained many epithelial cells with intense cytoplasmic staining
for cathepsin D while proximal segments showed a reduction in number of positively stained cells. By Day 7 post-castration,
cells in proximal segments, though atrophied, were devoid of staining for cathepsin D. |
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ISSN: | 0006-3363 1529-7268 |
DOI: | 10.1095/biolreprod43.6.1079 |